Job Title: Senior Clinical Research Coordinator
Location: Brentwood, TN 37027
Duration: 6 Months
Position Summary:
The Senior Clinical Research Coordinator manages multiple research protocols, liaises with investigators and site personnel, and ensures compliance and patient safety. The role involves coordinating assessments, documenting tasks, supporting site development, and training junior coordinators.
Major Responsibilities:
- Coordinate research protocols and operational activities.
- Liaise with sponsors, site teams, and IRB; manage schedules from feasibility to closeout.
- Document protocol tasks, correspondence, and data requests accurately.
- Ensure compliance with SOPs and protocol requirements.
- Support site feasibility, process development, and enrollment monitoring.
- Train CRC Levels I/II and act as a role model.
Must-Have Desired Traits/Experiences:
- Collaborative: Team-oriented, effective in cross-functional settings.
- Detail-Oriented: Meticulous in documentation and compliance.
- Adaptable: Thrives in dynamic environments with shifting priorities.
Education & Experience:
- Bachelor's degree (required); Master's degree (preferred).
- 1+ years of relevant experience (required); 5+ years (preferred).
- ACRP/CCRP certification (preferred).
Key Skills & Behaviors:
- Knowledge of ICH guidelines, CFR, and research terminology.
- Strong communication, organization, and time management.
- Clinical skills: ECG, phlebotomy, specimen handling.
- Self-motivated with a focus on quality and compliance.